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Nerve Ultrasound Protocol to Detect Dysimmune Neuropathies
Published on: October 7, 2021
Sarcoid polyneuropathy masquerading as chronic inflammatory demyelinating polyneuropathy
Neel S Singhal1, Viktoriya S Irodenko1, Marta Margeta2
1Department of Neurology, University of California San Francisco, 505 Parnassus Avenue, Box 0114, San Francisco, California, 94143, USA.
Sarcoid polyneuropathy can mimic chronic inflammatory demyelinating polyneuropathy (CIDP), posing a diagnostic challenge. Early diagnosis through biopsies is crucial for effective treatment of this rare neurological disorder.
Area of Science:
- Neurology
- Immunology
- Pathology
Background:
- Sarcoid polyneuropathy is an uncommon neurological disorder and a potential initial manifestation of sarcoidosis.
- It presents with diverse clinical features, making diagnosis difficult.
Observation:
- A 36-year-old male with a decade-long diagnosis of sensory-predominant chronic inflammatory demyelinating polyneuropathy (CIDP) showed limited response to immunosuppressants.
- He presented with gait disturbance and muscle cramps, with electrodiagnostic findings suggesting chronic demyelinating polyradiculoneuropathy and conduction blocks.
Findings:
- Systemic symptoms emerged, and tissue biopsies confirmed granulomatous disease, leading to a revised diagnosis of sarcoid polyneuropathy.
- The patient experienced symptom improvement following steroid therapy.
Implications:
- Sarcoid polyneuropathy diagnosis requires a high index of suspicion in atypical neuropathy cases.
- Nerve and muscle biopsies are vital for diagnosing this treatable condition, especially with refractory symptoms or systemic signs.
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